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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466333Generated: October 27, 2026

Chlorotrimethylgermane → 2-(3,5-Bis(trimethylgermyl)phenyl]-2-methyl-1,3-dioxolane

https://huagongshe.com/reaction/466333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylgermaneHCID 73723—
ReactantMagnesiumHCID 5462224—
Reactant2-(3,5-Dibromophenyl)-2-methyl-1,3-dioxolaneHCID 12884905—
SolventTetrahydrofuranHCID 8028—
Product2-(3,5-Bis(trimethylgermyl)phenyl]-2-methyl-1,3-dioxolaneHCID 1288490865%
Product2-(3-Trimethylgermylphenyl)-2-methyl-1,3-dioxolaneHCID 1460565411%

Reaction Steps

To a suspension of 108 mg (4.44 mmol) of magnesium and 765 mg (5.00 mmol) of trimethylgermyl chloride was added a solution of 644 mg (2.00 mmol) of 2-(3,5-dibromophenyl)-2-methyl-1,3-dioxolane in 10 ml of tetrahydrofuran at 40° C., stirred in an atmosphere of argon. The mixture was stirred at 70° C. for 4.5 hr. and at room temperature overnight. The reaction mixture was poured into ice-aqueous sodium bicarbonate solution and extracted with methylene chloride. The solvent was removed to give pale brown crystals, which were purified by column chromatography on silica gel [eluent: methylene chloride-n-hexane (1:1)] to give 514 mg (yield 65%) of 2-[3,5-bis(trimethylgermyl)phenyl]-2-methyl-1,3-dioxolane, m.p. 54° C., and 61 mg (yield 11%) of 2-(3-trimethylgermylphenyl)-2-methyl-1,3-dioxolane and 75 mg of the mixture, in which the ratio was 3:2 (by NMR).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155249
Source datasetuspto-grants-1992_10
ORD IDord-41bd66200ed74803aac1e8f5d1700a2a
Source noteuspto-grants-1992_10